MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Denys-Drash syndrome

ORPHA:220Disease
Autosomal dominant

Dermatitis herpetiformis

ORPHA:1656Disease
Not applicable

Dermatofibrosarcoma protuberans

ORPHA:31112Disease
Not applicable

Dermatoleukodystrophy

ORPHA:1659Disease
Autosomal recessive

Dermatomyositis

ORPHA:221Disease
Not applicable

Dermatoosteolysis, Kirghizian type

ORPHA:1657Malform.
Autosomal recessive

Dermatopathia pigmentosa reticularis

ORPHA:86920Disease
Autosomal dominant

Dermatosparaxis Ehlers-Danlos syndrome

ORPHA:1901Disease
Autosomal recessive

Dermochondrocorneal dystrophy

ORPHA:79149Disease
Autosomal recessive

Dermoid or epidermoid cyst of the central nervous system

ORPHA:530033Morph.

Dermoodontodysplasia

ORPHA:1660Malform.
Autosomal dominant

Dermotrichic syndrome

ORPHA:99688Malform.

Desbuquois syndrome

ORPHA:1425Malform.
Autosomal recessive

Desmin-related myopathy with Mallory body-like inclusions

ORPHA:84132Disease
Autosomal recessive

Desminopathy

ORPHA:98909Disease
Autosomal dominant, Autosomal recessive

Desmoid tumor

ORPHA:873Disease
Not applicable, Unknown

Desmoplastic infantile astrocytoma/ganglioglioma

ORPHA:251940Disease
Not applicable

Desmoplastic small round cell tumor

ORPHA:83469Disease
Not applicable

Desmoplastic/nodular medulloblastoma

ORPHA:251863Hist. sub.
Not applicable

Desmosterolosis

ORPHA:35107Disease
Autosomal recessive

Developmental and epileptic encephalopathy with spike-wave activation in sleep

ORPHA:725Disease
Autosomal dominant, Not applicable

Developmental and speech delay due to SOX5 deficiency

ORPHA:313892Clin. sub.
Autosomal dominant, Not applicable

Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency

ORPHA:289307Disease
Autosomal recessive

Developmental delay with autism spectrum disorder and gait instability

ORPHA:329195Disease
Autosomal recessive